Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1266141
Disease: Nephrogenic adenofibroma
Nephrogenic adenofibroma 		1 0 1 0.33 0 0
CUI: C1274943
Disease: Drug-induced panniculitis
Drug-induced panniculitis 		1 0 1 0.33 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis 		1 0 1 0.33 0 0
CUI: C1275419
Disease: Desmoplastic spindle and epithelioid cell melanocytic nevus of skin
Desmoplastic spindle and epithelioid cell melanocytic nevus of skin 		1 0 1 0.33 0 0
CUI: C1304321
Disease: Eruptive melanocytic nevi
Eruptive melanocytic nevi 		1 2 1 0.33 2 1.00
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma 		1 0 1 0.33 0 0
CUI: C1333802
Disease: Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract 		1 0 1 0.33 0 0
CUI: C1333826
Disease: Glomus Tumor of Uncertain Malignant Potential
Glomus Tumor of Uncertain Malignant Potential 		1 0 1 0.33 0 0
CUI: C1334222
Disease: Intermediate Risk Gastrointestinal Stromal Tumor
Intermediate Risk Gastrointestinal Stromal Tumor 		1 0 1 0.33 0 0
CUI: C1334720
Disease: Metastatic Malignant Peripheral Nerve Sheath Tumor
Metastatic Malignant Peripheral Nerve Sheath Tumor 		1 2 1 0.33 2 1.00
CUI: C1336056
Disease: Spindle Cell Type Gastrointestinal Stromal Tumor
Spindle Cell Type Gastrointestinal Stromal Tumor 		1 0 1 0.33 0 0
CUI: C1541333
Disease: adult acute myeloid leukemia with inv(16)(p13;q22)
adult acute myeloid leukemia with inv(16)(p13;q22) 		1 0 1 0.33 0 0
CUI: C1847874
Disease: PHACE association
PHACE association 		1 0 1 0.33 0 0
CUI: C1857534
Disease: Postnatal onset growth deficiency
Postnatal onset growth deficiency 		1 0 1 0.33 0 0
CUI: C2609093
Disease: Pancreatic neuroendocrine tumour metastatic
Pancreatic neuroendocrine tumour metastatic 		5 2 2 0.33 2 1.00
CUI: C2674636
Disease: GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL 		1 0 1 0.33 0 0
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
ASTROCYTOMA, LOW-GRADE, SOMATIC 		1 1 1 0.33 1 0.50
CUI: C2698309
Disease: B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged
B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged 		1 0 1 0.33 0 0
CUI: C2931518
Disease: Plexosarcoma
Plexosarcoma 		1 0 1 0.33 0 0
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		1 0 1 0.33 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 0.33 0 0
CUI: C3897744
Disease: recurrent childhood pleomorphic xanthoastrocytoma
recurrent childhood pleomorphic xanthoastrocytoma 		1 0 1 0.33 0 0
CUI: C3897746
Disease: recurrent childhood pilocytic astrocytoma
recurrent childhood pilocytic astrocytoma 		1 2 1 0.33 2 1.00
CUI: C4016294
Disease: PIEBALDISM WITH SENSORINEURAL DEAFNESS
PIEBALDISM WITH SENSORINEURAL DEAFNESS 		1 0 1 0.33 0 0
CUI: C4016297
Disease: PIEBALDISM, PROGRESSIVE
PIEBALDISM, PROGRESSIVE 		1 0 1 0.33 0 0